Trial of Selective Early Treatment of Patent Ductus Arteriosus with Ibuprofen

Gupta, Samir; Subhedar, Nimish V; Bell, Jennifer L; Field, David; Bowler, Ursula; Hutchison, Elizabeth; Johnson, Sam; Kelsall, Wilf; Pepperell, Justine; Roberts, Tracy; Sinha, Sunil; Stanbury, Kayleigh; Wyllie, Jonathan; Hardy, Pollyanna; Juszczak, Edmund; Baby-OSCAR Collaborative Group, Baby-OSCAR Collaborative Group

Abstract

BACKGROUND: The cyclooxygenase inhibitor ibuprofen may be used to treat patent ductus arteriosus (PDA) in preterm infants. Whether selective early treatment of large PDAs with ibuprofen would improve short-term outcomes is not known. METHODS: We conducted a multicenter, randomized, double-blind, placebo-controlled trial evaluating early treatment (≤72 hours after birth) with ibuprofen for a large PDA (diameter of ≥1.5 mm with pulsatile flow) in extremely preterm infants (born between 23 weeks 0 days' and 28 weeks 6 days' gestation). The primary outcome was a composite of death or moderate or severe bronchopulmonary dysplasia evaluated at 36 weeks of postmenstrual age. RESULTS: A total of 326 infants were assigned to receive ibuprofen and 327 to receive placebo; 324 and 322, respectively, had data available for outcome analyses. A primary-outcome event occurred in 220 of 318 infants (69.2%) in the ibuprofen group and 202 of 318 infants (63.5%) in the placebo group (adjusted risk ratio, 1.09; 95% confidence interval [CI], 0.98 to 1.20; P = 0.10). A total of 44 of 323 infants (13.6%) in the ibuprofen group and 33 of 321 infants (10.3%) in the placebo group died (adjusted risk ratio, 1.32; 95% CI, 0.92 to 1.90). Among the infants who survived to 36 weeks of postmenstrual age, moderate or severe bronchopulmonary dysplasia occurred in 176 of 274 (64.2%) in the ibuprofen group and 169 of 285 (59.3%) in the placebo group (adjusted risk ratio, 1.09; 95% CI, 0.96 to 1.23). Two unforeseeable serious adverse events occurred that were possibly related to ibuprofen. CONCLUSIONS: The risk of death or moderate or severe bronchopulmonary dysplasia at 36 weeks of postmenstrual age was not significantly lower among infants who received early treatment with ibuprofen than among those who received placebo. (Funded by the National Institute for Health Research Health Technology Assessment Programme; Baby-OSCAR ISRCTN Registry number, ISRCTN84264977.).

Citation

Gupta, S., Subhedar, N. V., Bell, J. L., Field, D., Bowler, U., Hutchison, E., Johnson, S., Kelsall, W., Pepperell, J., Roberts, T., Sinha, S., Stanbury, K., Wyllie, J., Hardy, P., Juszczak, E., & Baby-OSCAR Collaborative Group, B.-O. C. G. (2024). Trial of Selective Early Treatment of Patent Ductus Arteriosus with Ibuprofen. New England Journal of Medicine, 390(4), 314-325. https://doi.org/10.1056/NEJMoa2305582

• Journal Article Type: Article
• Acceptance Date: Nov 28, 2023
• Online Publication Date: Jan 25, 2024
• Publication Date: Jan 25, 2024
• Deposit Date: Nov 29, 2023
• Publicly Available Date: Jan 25, 2024
• Journal: New England Journal of Medicine
• Print ISSN: 0028-4793
• Electronic ISSN: 1533-4406
• Publisher: Massachusetts Medical Society
• Peer Reviewed: Peer Reviewed
• Volume: 390
• Issue: 4
• Pages: 314-325
• DOI: https://doi.org/10.1056/NEJMoa2305582
• Keywords: Humans, Ibuprofen - administration & dosage - adverse effects - therapeutic use, Bronchopulmonary Dysplasia - etiology - mortality, Infant, Extremely Premature, Double-Blind Method, Treatment Outcome, Time Factors, Cyclooxygenase Inhibitors - administration & dosage - adverse effects - therapeutic use, Ductus Arteriosus, Patent - complications - drug therapy - mortality, Infant, Newborn, Anti-Inflammatory Agents, Non-Steroidal - administration & dosage - adverse effects - therapeutic use
• Public URL: https://nottingham-repository.worktribe.com/output/27865025
• Publisher URL: https://www.nejm.org/doi/full/10.1056/NEJMoa2305582
• Additional Information: Authors on behalf of the Baby-OSCAR Collaborative Group.